Canonical Allele Identifier: CA456511018

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96191230T>G , CM000669.2:g.96191230T>G	GRCh38
NC_000007.13:g.95820542T>G , CM000669.1:g.95820542T>G	GRCh37
NC_000007.12:g.95658478T>G	NCBI36
NG_012247.1:g.135918A>C
NG_012247.2:g.135918A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014251.3:c.633A>C MANE Select	NP_055066.1:p.Thr211=
ENST00000265631.10:c.633A>C MANE Select	ENSP00000265631.6:p.Thr211=
NM_001160210.1:c.633A>C	NP_001153682.1:p.Thr211=
NM_001160210.2:c.633A>C	NP_001153682.1:p.Thr211=
NM_014251.2:c.633A>C	NP_055066.1:p.Thr211=
NR_027662.1:n.708A>C
NR_027662.2:n.659A>C
ENST00000265631.9:c.633A>C	ENSP00000265631.5:p.Thr211=
ENST00000416240.6:c.633A>C	ENSP00000400101.2:p.Thr211=
XM_006715831.2:c.666A>C	XP_006715894.1:p.Thr222=
XM_006715831.4:c.666A>C	XP_006715894.1:p.Thr222=
XM_011515727.1:c.666A>C	XP_011514029.1:p.Thr222=
XM_011515727.3:c.666A>C	XP_011514029.1:p.Thr222=
XM_017011663.1:c.624A>C	XP_016867152.1:p.Thr208=
XM_017011664.2:c.-126A>C	XP_016867153.1:n.-126A>C
XM_017011665.1:c.-126A>C	XP_016867154.1:n.-126A>C
XR_001744525.2:n.804A>C
XR_002956405.1:n.946A>C